Human Diseases in ICD-11 Classification

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 01 Certain infectious or parasitic diseases
 02 Neoplasms
 03 Diseases of the blood or blood-forming organs
 04 Diseases of the immune system
 05 Endocrine, nutritional or metabolic diseases
 06 Mental, behavioural or neurodevelopmental disorders
 07 Sleep-wake disorders
 08 Diseases of the nervous system
 09 Diseases of the visual system
 10 Diseases of the ear or mastoid process
 11 Diseases of the circulatory system
 12 Diseases of the respiratory system
 13 Diseases of the digestive system
 14 Diseases of the skin
 15 Diseases of the musculoskeletal system or connective tissue
 16 Diseases of the genitourinary system
 17 Conditions related to sexual health
 18 Pregnancy, childbirth or the puerperium
 19 Certain conditions originating in the perinatal period
 20 Developmental anomalies
   Structural developmental anomalies primarily affecting one body system
   Multiple developmental anomalies or syndromes
     LD20  Syndromes with central nervous system anomalies as a major feature
       H00530  Joubert syndrome
       H00897  Pontocerebellar hypoplasia
       H01001  COACH syndrome
       H01811  Arima syndrome
       H02272  CAPOS syndrome
       H02431  Cerebellar hypoplasia, epilepsy, and global developmental delay
       H00268  Lissencephaly
       H00792  Warburg micro syndrome
       H02117  Neu-Laxova syndrome
       H00616  Bowen-Conradi syndrome
       H00840  Band-like calcification with simplified gyration and polymicrogyria
       H00990  Microcephaly, Amish type
       H00991  Microcephalic osteodysplastic primordial dwarfism, type II (MOPD II)
       H00993  Microcephalic osteodysplastic primordial dwarfism, type I (MOPD I)
       H01872  Microcephaly-capillary malformation syndrome
       H01876  Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation
       H01921  MICPCH syndrome
       H02132  Microcephaly syndrome
       H02282  Spastic tetraplegia, thin corpus callosum, and progressive microcephaly
       H00544  Septo-optic dysplasia
       H00816  Agenesis of the corpus callosum with peripheral neuropathy
       H01034  L1 syndrome
       H01035  Corpus callosum, agenesis of, with mental retardation, ocular coloboma and micrognathia
       H01776  Aicardi syndrome
       H01789  You-Hoover-Fong syndrome
       H01919  Proud syndrome
       H01937  Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly
       H02366  Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome
       H02396  Corpus callosum agenesis with facial anomalies and cerebellar ataxia
     LD21  Syndromes with eye anomalies as a major feature
     LD22  Syndromes with dental anomalies as a major feature
     LD23  Syndromes with vascular anomalies as a major feature
     LD24  Syndromes with skeletal anomalies as a major feature
     LD25  Syndromes with face or limb anomalies as a major feature
     LD26  Syndromes with limb anomalies as a major feature
     LD27  Syndromes with skin or mucosal anomalies as a major feature
     LD28  Syndromes with connective tissue involvement as a major feature
     LD29  Syndromes with obesity as a major feature
     LD2A  Malformative disorders of sex development
     LD2B  Syndromes with premature ageing appearance as a major feature
     LD2C  Overgrowth syndromes
     LD2D  Phakomatoses or hamartoneoplastic syndromes
     LD2E  Syndromes with structural anomalies due to inborn errors of metabolism
     LD2F  Syndromes with multiple structural anomalies, without predominant body system involvement
     LD2G  Conjoined twins
     LD2H  Syndromic genetic deafness
     LD2Y  Other specified multiple developmental anomalies or syndromes
     LD2Z  Multiple developmental anomalies or syndromes, unspecified
   Chromosomal anomalies, excluding gene mutations
   LD90  Conditions with disorders of intellectual development as a relevant clinical feature
   LD9Y  Other specified developmental anomalies
   LD9Z  Developmental anomalies, unspecified
 21 Symptoms, signs or clinical findings, not elsewhere classified
 22 Injury, poisoning or certain other consequences of external causes

Last updated: November 21, 2020
ICD-11 by World Health Organization

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